BEUDAMED
    209 results · 23ms · Sources: EU EUDAMED, US FDA

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    Xario200G and Xario100G, Software V1.1 Diagnostic Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    Oticon

    FDA UDI
    Oticon A/S·05707131332837·OPN 2, KIT 312 2.4G NFM PB L C001

    ATRIUM GRADUATED WALL FLIXENE AX-BIFEM GRAFT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ULTRAEXTEND USWS-900A

    FDA 510(k)
    FDA Class 2 ·Radiology

    2182596-1997-00453

    FDA Adverse Event
    Injury ·Product code FTR·August 28, 1997

    2182596-1997-00452

    FDA Adverse Event
    Injury ·Product code FTR·August 28, 1997

    2182596-1997-00304

    FDA Adverse Event
    Injury ·Product code FTR·April 30, 1997

    2182596-1997-00296

    FDA Adverse Event
    Injury ·Product code FTR·April 30, 1997

    2182596-1997-00320

    FDA Adverse Event
    Injury ·Product code FTR·April 30, 1997

    2182596-1997-00328

    FDA Adverse Event
    Injury ·Product code FTR·April 30, 1997

    2182596-1997-00375

    FDA Adverse Event
    Injury ·Product code FTR·May 27, 1997

    2182596-1997-00329

    FDA Adverse Event
    Injury ·Product code FTR·April 30, 1997

    2182596-1996-00056

    FDA Adverse Event
    Injury ·Product code FTR·December 31, 1996

    2182596-1997-00090

    FDA Adverse Event
    Injury ·Product code FTR·March 3, 1997

    2182596-1997-00105

    FDA Adverse Event
    Injury ·Product code FTR·March 3, 1997

    2182596-1997-00088

    FDA Adverse Event
    Injury ·Product code FTR·March 3, 1997

    2182596-1997-00102

    FDA Adverse Event
    Injury ·Product code FTR·March 3, 1997

    2182596-1997-00089

    FDA Adverse Event
    Injury ·Product code FTR·March 3, 1997

    2182596-1997-00104

    FDA Adverse Event
    Injury ·Product code FTR·March 3, 1997

    2182596-1997-00107

    FDA Adverse Event
    Injury ·Product code FTR·March 3, 1997